Eu Ivdr Eu Ivd Class B On The Market

IDS-iSYS 17-OH Progesterone

Devices (same UDI-DI)
2
Certificates
0
Countries
32
Notified Bodies
0

Basic Information

Primary DI
05060169690738
Basic UDI-DI Code
5060169690738XP
Reference
IS-5100
Device Types
None provided
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market

Additional Description

The IDS-iSYS 17-OH Progesterone assay is an in vitro diagnostic device intended for the quantitative determination of 17-OH Progesterone in human serum or plasma on the IDS system. Results are to be used as an aid in the diagnosis and treatment of various disorders of the adrenal glands or the ovaries.

CND Nomenclature Codes

Code Description
W0102050106 PROGESTERONE

Available In Countries

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇾 Cyprus 🇨🇿 Czechia 🇩🇪 Germany 🇩🇰 Denmark 🇪🇪 Estonia 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇭🇷 Croatia 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇸 Iceland 🇮🇹 Italy 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden 🇸🇮 Slovenia 🇸🇰 Slovakia 🇹🇷 Türkiye 🇬🇧 United Kingdom

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